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HRID 332643作成日:2026年10月25日

1,4-Cyclohexadiene → (R)-5-(2-Amino-1-((tert-butyldimethylsilyl)oxy)ethyl)-8-hydroxyquinolin-2(1H)-one

https://huagongshe.com/reaction/332643

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-CyclohexadieneHCID 12343—
反応物(R)-5-(2-Azido-1-((tert-butyldimethylsilyl)oxy)ethyl)-8-(benzyloxy)quinolin-2(1H)-oneHCID 58505233—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物(R)-5-(2-Amino-1-((tert-butyldimethylsilyl)oxy)ethyl)-8-hydroxyquinolin-2(1H)-oneHCID 5902360487%

反応手順

To an ice-cooled suspension of (R)-5-(2-azido-1-(tert-butyldimethylsilyloxy)-ethyl)-8-(benzyloxy)quinolin-2(1H)-one (5.77 g, 12.8 mmol) and palladium on activated charcoal (5.8 g, 10% w/w wet) in ethanol (50 mL), 1,4-cyclohexadiene (12.0 mL, 126 mmol) was added dropwise. After stirring at this temperature for 30 minutes, the coolant was removed and replaced with a water bath at 30° C. The reaction was stirred at this temperature for 1 hour. The suspension was filtered and the filter cake washed with further ethanol. The filtrate was evaporated under reduced pressure to dryness. The resulting solid was suspended in acetonitrile and stirred for 1 hour. The suspension was filtered and the resulting solid air-dried under vacuum to afford the title compound (2.90 g, 87%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08877774B2
出典データセットuspto-grants-2014_11
ORD IDord-359cca3e08c349849edd45fa4617420c
出典メモuspto-grants-2014_11